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GGAGGACCCTAGTCCAGAGACTTTT[C/T]GGCTGAGGTTTCGGCAGTTCCGCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
GS1-259H13.2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
GS1-259H13.2 - transmembrane protein 225-like | ||||||
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There are no transcripts associated with this gene. |
ZSCAN25 - zinc finger and SCAN domain containing 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145115.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | NP_660090.2 | |
XM_005250194.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_005250251.1 | |
XM_011515905.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_011514207.1 | |
XM_011515906.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_011514208.1 | |
XM_011515907.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_011514209.1 | |
XM_011515908.2 | 706 | UTR 5 | XP_011514210.1 | |||
XM_011515909.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_011514211.1 | |
XM_011515910.2 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_011514212.1 | |
XM_017011824.1 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_016867313.1 | |
XM_017011825.1 | 706 | UTR 5 | XP_016867314.1 | |||
XM_017011826.1 | 706 | UTR 5 | XP_016867315.1 | |||
XM_017011827.1 | 706 | Missense Mutation | CGG,TGG | R,W 42 | XP_016867316.1 |